Is MSH3 p.Ser220Pro (c.658T>C) pathogenic?

MSH3 p.Ser220Pro (c.658T>C) is classified Uncertain significance in MSH3 (ClinVar, Single submitter, 1 submitter; last evaluated 2021-06-16). AlphaMissense: likely benign (0.0462); Absent from gnomAD v4.1.

How common is MSH3 p.Ser220Pro (c.658T>C) in the general population?

MSH3 p.Ser220Pro (c.658T>C) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about MSH3 p.Ser220Pro (c.658T>C)?

AlphaMissense predicts likely benign (score 0.0462) — an in-silico prediction, not a clinical call.

MSH3 p.Ser220Pro

c.658T>C · rs2112812220 · VCV1433791

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.0462 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.0462	likely benign
REVEL	0.188	benign-leaning
SaProt	LLR -6.45	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP -0.15	GERP -2.2
Regional constraint	o/e 1.08	unconstrained · MANE · 221 kb · p 0.0024 · regional, not allelic
Overall
CADD	4.15	PHRED · no single calibrated threshold — expert panels disagree

ClinVar classifies this uncertain; the computational predictors unanimously lean tolerated — a triage signal, not a reclassification

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: MSH3
Protein: p.Ser220Pro
Coding: c.658T>C
MANE Select: NM_002439
dbSNP: rs2112812220
Type: single nucleotide variant
Location: chr5:80670175 (GRCh38)
Gene constraint: LOEUF 1.027 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 79.48 · 25 PDB
Residue 220: the 'interaction with exo1' region; a β-strand; the 'disordered' region

Full MSH3 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

MSH3 p.Ser220Leu Uncertain significance ★★ ⚠ same residue
MSH3 p.Ser220= Likely benign ★★ same residue
MSH3 p.Ser220Ter Pathogenic ★ same residue
MSH3 p.Ser220Ala Uncertain significance ★ ⚠ same residue
MSH3 p.Ser220Thr Uncertain significance ★ ⚠ same residue
MSH3 c.1341-2A>C Likely pathogenic ★★ same type
MSH3 c.1341-2A>G Likely pathogenic ★★ same type
MSH3 c.1568+1G>A Likely pathogenic ★★ same type

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/msh3-p-ser220pro (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown